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Updated: Aug 8, 2026

Two Methods of Heterokaryon Formation to Discover HCV Restriction Factors
Published on: July 16, 2012
[Hepatitis C and immunoglobulin heavy-chain gene rearrangement]
Beáta Gasztonyi1, Alajos Pár, László Kereskai
1I. sz. Belgyógyászati Klinika, Pécsi Tudományegyetem, Altalános Orvostudományi Kar.
Insights
Immunoglobulin heavy chain (IgH) gene rearrangement in Hepatitis C virus (HCV) positive patients may indicate lymphoproliferative disorders. This finding supports the link between HCV infection, B-cell proliferation, and lymphoma development.
Area of Science:
- Hepatology and Immunology
- Molecular Biology
- Oncology
Context:
- Hepatitis C virus (HCV) infection affects not only hepatocytes but also salivary glands, peripheral blood monocytes, and lymphoid cells, contributing to systemic manifestations.
- HCV infection triggers B-cell and T-cell activation, immune response modulation, and lymphoproliferation, potentially leading to B-cell non-Hodgkin's lymphoma (NHL).
- Immunoglobulin heavy chain (IgH) and light chain (IgL) gene rearrangements are characteristic of B-cell NHLs, appearing early in their development.
Purpose:
- To investigate the presence and significance of IgH gene rearrangements in patients with chronic Hepatitis C virus (HCV) infection.
- To explore the association between IgH gene rearrangements, cryoglobulinemia, and lymphoproliferative disorders in HCV-positive individuals.
Summary:
- Immunoglobulin heavy chain (IgH) gene rearrangements were analyzed in sera from 57 chronic HCV patients and 11 HCV-positive cryoglobulinemic patients.
- Cryoglobulinemia was present in 20% of chronic HCV patients. IgH rearrangement was detected in 10.29% of all patients, with 57.14% of those with IgH rearrangement also having cryoglobulinemia.
- The study found that IgH gene rearrangement in HCV-positive patients can serve as an indicator of lymphoproliferative disorders, supporting the role of HCV in B-cell proliferation and subsequent lymphoma development.
Impact:
- These findings reinforce the hypothesis linking IgH gene rearrangement in HCV-positive individuals to lymphoproliferative disorders.
- The study highlights the potential of IgH rearrangement analysis as a diagnostic marker for HCV-associated B-cell proliferation and lymphoma risk.
- Understanding this association may lead to improved monitoring and earlier detection of B-cell malignancies in patients with chronic HCV infection.
Unlabelled:
Hepatitis C virus (HCV) has cytopathogenic effect not only on hepatocytes, however on salivary glands, monocytes of peripheral blood and lymphoid cells, may explain the systemic manifestations of the infection. HCV activates B and T-cells, modifies the immune response, causes lymphoproliferation, leading the development of B-cell non-Hodgkin's lymphoma (NHL). In the majority of B-cell NHLs immunoglobulin heavy chain (IgH) and light chain (IgL) genes are rearranged and expressed on cell surface in the early stage of the ontogenesis. The analyses of IgH rearrangement prove the clonality of lymphoproliferative disorders giving a powerful approach to the B-cell origin identification of cell proliferation.
Patients And Methods:
IgH gene rearrangements were examined from the sera of 57 chronic HCV infected patients and 11 HCV-positive cryoglobulinemic patients as well.
Results:
Cryoglobulinemia was detected in 20% of all chronic hepatitis C virus infected patients and IgH rearrangement was observed in 10.29% (7/68), 4/7 patients (57.14%) suffered from cryoglobulinemia.
Conclusions:
These results support the hypothesis that IgH gene rearrangement in HCV positive patients can indicate the lymphoproliferative disorder in the HCV infection released B-cell proliferation and lymphoma development.
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